# autosomal dominant nonsyndromic deafness 11

> autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life with a flat or gently downsloping audioprofiles and has material basis in mutation in the MYO7A gene on chromosome 11q13

**Wikidata**: [Q28024670](https://www.wikidata.org/wiki/Q28024670)  
**Source**: https://4ort.xyz/entity/autosomal-dominant-nonsyndromic-deafness-11


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)